The QA Manager works closely with other internal department managers and supervisors to assure compliance with regulatory and Customer requirements. The position involves management of Document Control, Auditors, Production Control and Compliance. To work with all Supervision and employees to ensure that cGMP's, SQF 2000 and Praxis SOP's, Policies and Work Instructions are being followed.
Other duties may include, but are not limited to:
1. Assures compliance with the requirements of 21 CFR Part 211
2. Submit weekly Quality Activity reports to VP of Quality
3. Review Policies, SOP's, WI's, and Forms as required
4. Provide Quality coverage to all Praxis sites (Grand Rapids, MI & Columbus, OH)
5. Serves as backup for the VP of Quality in all matters related to Quality and Compliance
6. Provide training to all locations on QA related topics
7. Partner with HR for employee counseling, discipline, promotion, etc.
8. Continually work to improve the effectiveness of the quality management system through the use of quality policy, quality objectives, audit results, analysis of data and corrective and preventative actions
9. 25% travel
Eduacation, Skills & Experience Required:
1. 5+ years progressive responsibility in Quality Management - GMP manufacturing (Pharmaceutical & Holding Human Food) environment preferred
2. Bachelor's degree in applicable field of study
3. Strong investigative abilities
4. Effective communication skills, both verbal and written
5. Ability to effectively present training to small or medium sized groups
Please visit here to apply online.
Other duties may include, but are not limited to:
1. Assures compliance with the requirements of 21 CFR Part 211
2. Submit weekly Quality Activity reports to VP of Quality
3. Review Policies, SOP's, WI's, and Forms as required
4. Provide Quality coverage to all Praxis sites (Grand Rapids, MI & Columbus, OH)
5. Serves as backup for the VP of Quality in all matters related to Quality and Compliance
6. Provide training to all locations on QA related topics
7. Partner with HR for employee counseling, discipline, promotion, etc.
8. Continually work to improve the effectiveness of the quality management system through the use of quality policy, quality objectives, audit results, analysis of data and corrective and preventative actions
9. 25% travel
Eduacation, Skills & Experience Required:
1. 5+ years progressive responsibility in Quality Management - GMP manufacturing (Pharmaceutical & Holding Human Food) environment preferred
2. Bachelor's degree in applicable field of study
3. Strong investigative abilities
4. Effective communication skills, both verbal and written
5. Ability to effectively present training to small or medium sized groups
Please visit here to apply online.
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